Scientific Protein Laboratories, LLC
On-Site QA Specialist
Scientific Protein Laboratories, LLC, Waunakee, Wisconsin, United States, 53597
Overview
Join our team as an On-Site QA Specialist at Scientific Protein Laboratories, LLC (SPL), a world leader in biosourced pharmaceuticals, located just outside of Madison, Wisconsin in Waunakee. SPL specializes in the development and cGMP compliant manufacturing of Active Pharmaceutical Ingredients (APIs). This on-site role supports Quality Assurance responsibilities on-site. Responsibilities
Assist all departments in the identification and evaluation of facility events; ensure proper documentation is initiated to capture the event. Review executed batch records. Inspect and disposition raw materials based on approved specifications. Write deviations, investigations, change controls and/or CAPAs. Perform shipping release procedures. Assist in the preparation of Annual Product Review documentation for all SPL marketed products. Provide administrative support for the on-site QA department (e.g., generation of DCRs, file organization, data compilation, training activities). Qualifications
Education: Bachelor’s degree or above required; bachelor’s degree or above in a scientific discipline preferred. Experience: 2+ years of experience required; 5+ years of experience preferred. Position will be filled up to the mid-level and determined at the discretion of the hiring manager. Why Join SPL
Our employees are our success! We recruit motivated people, recognize their contributions, and support their development to reach their full potential. Perks include: competitive compensation; excellent benefits package (Medical, Dental and Vision on Day 1; Life and AD&D Insurance; Short and Long-term Disability); Health and Flexible Saving Account options; Employee Assistance Program; generous vacation; paid Holidays; 401k; advancement opportunities; team-oriented environment; community involvement; company events and more. SPL is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Employment Details
Seniority level: Entry level Employment type: Other Job function: Quality Assurance Industries: Pharmaceutical Manufacturing Note: This description reflects the responsibilities, qualifications, and expectations for the On-Site QA Specialist role at SPL and may include boilerplate statements that are standard for job postings.
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Join our team as an On-Site QA Specialist at Scientific Protein Laboratories, LLC (SPL), a world leader in biosourced pharmaceuticals, located just outside of Madison, Wisconsin in Waunakee. SPL specializes in the development and cGMP compliant manufacturing of Active Pharmaceutical Ingredients (APIs). This on-site role supports Quality Assurance responsibilities on-site. Responsibilities
Assist all departments in the identification and evaluation of facility events; ensure proper documentation is initiated to capture the event. Review executed batch records. Inspect and disposition raw materials based on approved specifications. Write deviations, investigations, change controls and/or CAPAs. Perform shipping release procedures. Assist in the preparation of Annual Product Review documentation for all SPL marketed products. Provide administrative support for the on-site QA department (e.g., generation of DCRs, file organization, data compilation, training activities). Qualifications
Education: Bachelor’s degree or above required; bachelor’s degree or above in a scientific discipline preferred. Experience: 2+ years of experience required; 5+ years of experience preferred. Position will be filled up to the mid-level and determined at the discretion of the hiring manager. Why Join SPL
Our employees are our success! We recruit motivated people, recognize their contributions, and support their development to reach their full potential. Perks include: competitive compensation; excellent benefits package (Medical, Dental and Vision on Day 1; Life and AD&D Insurance; Short and Long-term Disability); Health and Flexible Saving Account options; Employee Assistance Program; generous vacation; paid Holidays; 401k; advancement opportunities; team-oriented environment; community involvement; company events and more. SPL is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Employment Details
Seniority level: Entry level Employment type: Other Job function: Quality Assurance Industries: Pharmaceutical Manufacturing Note: This description reflects the responsibilities, qualifications, and expectations for the On-Site QA Specialist role at SPL and may include boilerplate statements that are standard for job postings.
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